VERSABOND AB 40 GRAMS FORMULATION 2 (2020-12-18)

Starting date:

December 18, 2020

Posting date:

December 31, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-74689

Last updated:
2020-12-31

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  Reason
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  Affected products

Affected Products 

VERSABOND AB 40 GRAMS FORMULATION 2

Reason

Smith+Nephew has initiated a field action to remove a single lot of Versabond AB 40 Grams Formulation 2 due to potential heat and humidity exposure. It was reported that the affected lot contained an atypical sandy, flaky or grainy consistency when mixing.

Affected products